Jandron

Boy, Age: 1

Primary Diagnosis: Epilepsy/ seizure disorder, Other Special Needs

Listed: Apr 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

(Information is from January 2026 when Jandron was 10 months old. He was born in late February 2025)

Jandron was born 5 weeks prematurely to a 20-year-old mother into a highly vulnerable situation. At birth, he experienced respiratory distress syndrome, requiring mechanical ventilation. Jandron has ongoing medical diagnoses of moderate bronchopulmonary dysplasia and recurrent post-viral wheezing, making him dependent on supplemental oxygen. He also has epilepsy, mild encephalopathy, and horizontal nystagmus (involuntary eye movement). Jandron has a history of hospitalizations to treat seizures, bronchiolitis, and wheezing. To manage his health, he takes several daily medications.

Even with his medical issues, Jandron shows beautiful developmental progress–not to mention a BEAUTIFUL smile under the sticker we had to place over his picture. He displays fluid and spontaneous movements of his arms and legs. While he has slight hypotonia (low muscle tone) in his trunk, he successfully rolls from his back to his stomach on his right side. He is also beginning to practice fine motor skills, occasionally using a pincer grip to explore the world around him. He is finding his voice, frequently emitting sweet vowel and syllabic sounds. His responses to auditory stimuli are becoming increasingly consistent. He is a curious observer. He pays close attention to his environment, shows great curiosity toward objects, and responds positively to simple stimuli. He makes wonderful eye contact with his caregivers and rewards them with warm smiles. As a 10-month-old infant with medical needs, he requires full assistance for all daily living and basic hygiene activities.

Jandron is a gentle child with a mostly calm and receptive temperament. Because of his young age and medical history, he relies entirely on his caregivers for emotional regulation. He clearly expresses his feelings, including showing displeasure, and communicates his basic needs through facial expressions and crying. He demonstrates a healthy, positive attachment style with his current caregivers. Jandron seeks connection and instantly calms down when given physical contact and comfort. His ability to connect, look into your eyes, and accept soothing touch shows a profound resilience and a readiness to bond with a permanent family.

While he is too young for traditional hobbies, he has clear preferences that highlight his unique personality. He is an attentive little boy who loves to watch the world around him. He shows a distinct interest in exploring objects with his hands and listening to the sounds in his environment. Above all, his favorite place to be is in the arms of someone who cares for him. He loves physical touch, gentle holding, and the reassurance of a loving voice. He needs a family that is highly sensitive to his medical diagnoses, but more importantly, a family that will cherish his smiles, celebrate his milestones, and offer him the safe, warm home he deeply deserves.

Tio

Boy, Age: 1

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Congenital Heart Defect

Listed: Apr 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Trust me, I’m cute under this sticker they put on my face!

Here is what is said about me:

Tio was born 4 weeks prematurely with a complex congenital heart condition, including pulmonary atresia and Tetralogy of Fallot. He has undergone multiple cardiac surgeries, including right ventricle-to-pulmonary artery conduit placement and angioplasty with stent placement. He has experienced postoperative complications, including surgical site infection and respiratory infections, all of which were medically managed. He currently requires continuous oxygen support via nasal cannula (1 liter per minute) and takes cardiac medications including furosemide, spironolactone, and low-dose aspirin. He remains under close pediatric and cardiology follow-up, with additional evaluations pending in genetics and general pediatrics.

Despite his significant medical history, Tio is described as a calm, affectionate, and resilient child. He responds warmly to caregivers, makes eye contact, smiles socially, and enjoys music, light-up toys, and physical closeness. He demonstrates curiosity about his environment and enjoys sensory exploration.

Developmentally, Tio presents global developmental delay secondary to his complex medical condition and prolonged hospitalizations. He can sit independently, roll, assume a crawling position, and manipulate objects with his hands. His fine motor skills are emerging, though slightly below expectations. Expressively, he babbles and produces repetitive syllables, though language development is delayed for his age. He receives ongoing interdisciplinary services including physical therapy, speech therapy, and psychological support. With continued therapeutic intervention and a stable family environment, he is expected to continue progressing.

Nutritionally, Tio is stable and well nourished, with adequate weight and height for age. His vaccination schedule is up to date. He tolerates solid foods well and maintains appropriate daily intake. Emotionally and socially, Tio forms attachments and responds positively to consistent caregiving. He expresses joy through smiles and gestures, communicates needs through crying and vocalization, and is receptive to affection. He has shown increasing emotional security and regulation within the structured environment of his current placement.

Tio would benefit from an adoptive family that is emotionally sensitive, patient, and well-prepared to manage complex medical needs. His family should be committed to ongoing cardiology care, therapeutic follow-up, and providing structured routines with nurturing support. A family with strong advocacy skills and access to pediatric cardiology services will be essential to meet his ongoing medical needs. Most importantly, he needs a loving, stable home that will encourage his development at his own pace and celebrate his resilience and strengths.

Tio is a gentle, sweet, and determined child whose smile reflects his strong will to live and connect. With proper medical care and the unconditional love of a permanent family, he has significant potential to thrive.

Ezekiel

Boy, Age: 2

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Genetic Condition (non-DS), Global developmental delays

Listed: Apr 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Ezekiel was born to a teenage mother whose family faced socioeconomic struggles including overcrowding, poor housing conditions, and a lack of access to basic needs. While his biological mother and grandmother tried to care for him, they lacked the resources and knowledge to meet his specific needs. When Ezekiel was just two months old, health workers noticed he was receiving improper nutrition, such as being fed gelatin from a bottle, and he was taken into care.

Ezekiel primary diagnoses include a genetic condition called Mosaic 1q21.1q22 duplication syndrome, microcephaly, and congenital hypotonia. He also has vision conditions, including optic atrophy and right convergent strabismus (a turned eye). A significant part of Ezekiel’s daily care revolves around his feeding. He has an infantile feeding and swallowing disorder. Because he cannot safely tolerate solid foods, he requires a specialized liquid and purée diet. He needs to eat while sitting at a 90-degree angle, offering thick textures and liquids from a spoon to protect his airway. Despite these challenges, his nutritional status is currently stable. He maintains a healthy weight for his height. He takes a daily iron supplement and actively participates in physical, occupational, and speech therapies. He will need ongoing care from a team of specialists, including genetics, gastroenterology, neuropediatrics, and ophthalmology.

Because of his genetic condition and low muscle tone, Ezekiel experiences significant global developmental delays. Although he is 18 months old chronologically, his developmental milestones currently align with those of a 5- to 6-month-old infant. He requires constant supervision and full support for all daily activities. His motor skills are slowly progressing with the help of his physical therapies, but his hypotonia affects his ability to move independently. His communication is primarily non-verbal, relying on expressions and sounds to connect with his caregivers. With consistent therapy and a structured environment, Ezekiel continues to show steady, beautiful progress at his own pace.

Ezekiel has a remarkably calm, happy, and gentle temperament. In his current foster home, he has formed strong, secure emotional bonds. He finds true refuge, acceptance, and security in the presence of the people who care for him. He manages his emotions well when he feels safe. Ezekiel thrives on physical affection and gentle reassurance. He shows a wonderful sense of confidence and relaxation when his trusted caregivers are nearby. He is an exploratory and willing child who embraces the world around him as long as he feels emotionally supported.

Ezekiel is a delightful little boy who finds joy in the simple things. He loves discovering his own body and spends time happily playing with his hands and feet. He enjoys it when adults and other children play with him, and he loves hearing the familiar voices of his foster family. He is a big fan of animal sounds and enjoys watching colorful shows like Paw Patrol, La Granja de Zenón, and La Vaca Lola. He also loves listening to children’s music. Mornings are a special time for Ezekiel because he absolutely loves taking baths, followed by relaxing gentle massages. He also enjoys going out, looking through car windows, and visiting cool, air-conditioned places like the grocery store.

When it comes to his special diet, Ezekiel has a great appetite! His absolute favorite meals are smooth purées made from beans, spinach, or arracacha mixed with chicken. For a sweet treat, he loves natural fruit compotes made from mango, banana, and apple.

Ezekiel needs a family that can embrace his medical routine while celebrating his beautiful spirit.

Rowand #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder

infantile cerebral palsy – spastic quadriparesis, severe degree; localized symptomatic epilepsy – secondarily generalized seizures; pronounced cerebellar atrophy; atrophy of the large cerebral hemispheres; pseudobulbar paresis; microcephaly; craniosynostosis; optic nerve atrophy; microphthalmia on the left; arachnoid brain cyst with communicating hydrocephalus and atrophy of the temporal lobes; delays in physical, motor, and neuropsychological development; severe mental delay

Listed: Mar 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Precious Rowand is a boy with complex special needs who is in need of a dedicated family able to provide him with the love, attention, specialized care, and therapies he requires.

Rowand remains in a lying position and is motor-passive. He tolerates interactions – tactile, verbal, musical. He does not initiate interaction when he is awake but remains calm. The boy reacts by crying in moments of discomfort. He reacts to sounds and movement around him.

Rowand is fully dependent on the care of adults. He requires constant specialized care for feeding (via NG tube), body positioning, and systematic motor rehabilitation.

Galen

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Down syndrome

Listed: Feb 2026

*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Galen is a lively and active boy. He lives with a supportive foster family and expresses affection through warm hugs and enthusiastic applause. As a family, they enjoy spending time together on walks to the river, watching movies, and swimming. Galen is especially drawn to bright, colorful toys with auditory features. When he hears music from his favorite genre, he joyfully waves his arms and taps his feet to the rhythm. Galen currently receives physical and occupational therapy services in the home. Galen communicates using nonverbal cues to express himself and indicate his wants and needs. Although he may be shy when first meeting new people, he builds meaningful connections through play, games, and shared toys. Contact Gladney for more information about Galen!

The listing agency has an additional $1000 grant to reduce the adoption fees for Galen, too!

Hendrix and Kody #

Sibling Group

Ages: 11, 11

Region: Eastern Europe

Primary Diagnosis: Behavior, Other Special Needs

Listed: Feb 2026

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Single Fathers, Available to Single Mothers, Siblings

Hendrix: prematurity; microcephaly; myopia; hypermetropia; astigmatism; amblyopia due to anopsia; polydactyly (6 fingers on the left hand – additional thumb); mild mental delay, significant disturbance of behavior requiring care or treatment.

Kody: prematurity; attachment disorder – disinhibited type, in a child with low stimulation

Johnny #

Boy, Age: 2

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Special needs: hydrocephalus – implanted ventriculoperitoneal shunt; macrocephaly; round hemangioma in the scalp area; intermittent convergent strabismus; phimosis; delayed neuropsychological development.

Listed: Feb 2026

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Meet precious Johnny! He is only 1 years old, turning 2 in the spring. Because of his special needs, he was never raised by his biological family and has spent his entire young life in the neonatology unit, in a children’s home, and now in his current group home for children with medical needs. Johnny is a gentle, sweet boy who needs a loving and devoted family.

Johnny can sit independently and he can assume a hands-and-knees position. He grasps toys and responds with positive emotion during interaction. He has good hand-to-mouth coordination. Johnny can turn from back to belly and vice versa. When standing, he has weak support on his legs.

Most of the time, Johnny is calm; there are no signs of increased anxiety, frustration, or aggression. He uses crying to seek attention or to satisfy needs but calms down quickly when comforted through hugging, gentle stroking, or talking. His sleep is calm.

Dane #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Autism

Listed: Feb 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

He has lived in a foster family since 6 months of age and requires constant supervision due to young age and behavioral challenges. He was diagnosed with childhood autism in June 2025.

He demonstrates a global developmental delay affecting physical, cognitive, emotional, and social functioning. Physical development shows a mild delay: he sits independently, stands up on his own, and walks with hand support. Fine and gross motor skills are slightly delayed; muscle tone is adequate, and there are no musculoskeletal disorders.

Neurologically and behaviorally, Dane shows limited social engagement: he does not respond to his name, does not maintain eye contact, does not follow commands, and does not initiate interaction. Play is non-functional and stereotypical (e.g., spinning objects). He exhibits stereotyped behaviors and requires adult guidance for constructive play.

Expressive speech is absent, with only incomprehensible vocalizations and occasional syllables. Cognitive functioning, memory, and intellect are below age level, and higher mental activity cannot be reliably assessed due to age and developmental limitations.

Emotionally, he is generally calm, responds to positive and negative stimuli with a delayed reaction, and shows attachment through hugging familiar caregivers. He rarely expresses needs verbally and may become distressed when objects are taken away.

Axton #

Boy, Age: 2

Primary Diagnosis: Congenital Heart Defect, Craniofacial disorder, Global developmental delays

Special needs: prematurity (2nd degree); low birth weight (1,560 g); microcephaly; congenital bilateral cleft lip and cleft palate (status post plastic surgery); congenital duodenal atresia (status post surgical correction); delayed neuropsychological development.

Listed: Feb 2026

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Meet adorable Axton! Axton has never lived with his biological family and has spent his entire life in hospitals and children’s institutions. His special needs are primarily medical, and his congenital malformations have been successfully treated surgically. Although his neuropsychological and motor development are delayed, Axton is making steady progress.

Axton moves around using a walker and is very active. He sits independently without support. His speech is in the process of development; he pronounces individual sounds and produces a variety of vocalizations.

Axton is cheerful and smiles often. He actively seeks the attention of adults and laughs out loud during playful interactions. He shows good adaptation to new environments and daily routines. Axton is calm and does not display self-aggressive behavior. He independently reaches for toys placed around him, taps them, and explores them with curiosity.

Axton is fed with a spoon by an adult while seated in a high chair. Efforts are being made to teach him to drink liquids from a cup. He falls asleep in a crib, and his sleep is calm.

Kenny

Boy, Age: 2

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Congenital Heart Defect, Down syndrome

Down syndrome, surgically corrected congenital heart disease , generalized hypotonia, glycion disorder with gastrostomy management, congenital hypothyroidism, malnutrition in correction, and global developmental delay with impairment in the motor, cognitive, language and social areas

Listed: Jan 2026

*** I am eligible for an additional $2,500 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome under the age of 6 are eligible for this grant. ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Kenny enjoys spending time in his children’s jumper which comes with various sensory stimulation accessories, as well as his crib. He is happy with physical contact, having movements made in his legs, and being lifted up. He has physical, occupational, and speech therapies 3 time a week. Kenny has achieved a notable improvement in his nutritional status. He needs an adoptive family with high emotional, affective, and physical availability, who has a solid support network and preferably experience in the care of children with special needs. It is essential that this family is committed to the active management of the health, therapeutic, and educational services that Kenny requires.

NEW VIDEOS:
https://vimeo.com/manage/videos/1151669660
https://vimeo.com/manage/videos/1151669587
Password: Adoptmaa

There is a $1,000 agency fee reduction for Kenny’s adoption via a specific agency.

Milo #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder, Global developmental delays

Listed: Dec 2025

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Chronic herpes simplex type 2 encephalitis. Microcephaly. Symptomatic epilepsy. Cerebral palsy – severe quadriparetic syndrome. Profound cognitive delay. Convergent concomitant strabismus. Nystagmus. Atopic dermatitis

Yoshi

Boy, Age: 4

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Congenital Heart Defect, Other Special Needs, Speech Delay

Neurodevelopmental delay, macrocephaly, muscular hypotrophy, growth concerns, expressive language disorder, and cardiac concerns

Listed: Dec 2025

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Information is from June 2025:

Yoshi was removed from his family at a young age, due to their lack of ability to provide adequate care. Yoshi presents with a complex medical profile requiring ongoing attention and care. His primary diagnoses include: Neurodevelopmental delay: affecting various areas of growth; Macrocephaly: disproportion of the skull/face and minor facial dysmorphisms; Muscular Hypotrophy: specifically noted in the lower extremities, though they are symmetrical; Growth Concerns: short stature and low weight, previously hospitalized for protein-calorie malnutrition; Expressive Language Disorder: significant difficulties in verbal communication; Cardiac Concerns: possible pulmonary valve insufficiency and mild tricuspid insufficiency (syndrome under study). He has a history of hospitalization for respiratory infections (pneumonia) and malnutrition but has stabilized under current care. He has no known allergies. His current medical regimen includes nutritional support. His vaccination schedule is up to date for his age.

Yoshi faces several developmental challenges. He exhibits a significant delay in verbal expression. His vocabulary is limited, and he struggles with pronunciation, articulation, and structuring sentences. He primarily uses gestures and short words to communicate. While he has shown improved mobility, he experiences difficulties with gross motor skills such as running, jumping, and climbing stairs. He exhibits generalized hypotonia and issues with balance and coordination. He has cognitive difficulties understanding complex instructions. He is currently working on sphincter control and still requires diapers. However, he is showing progress in independence, such as using a spoon during meals.

Despite his challenges, Yoshi possesses a warm and engaging personality. He is described as an active, affectionate, and receptive child. He shows a genuine interest in social interaction and engaging with the world around him. Yoshi has an adequate capacity to form bonds with significant adults and is progressively learning to interact with peers. He enjoys group play and is capable of sharing toys. He tends to express his emotions clearly through facial expressions and gestures. He thrives in environments where he feels emotionally secure.

Yoshi is a child with distinct likes and dislikes that help define his daily life: He has a strong preference for symbolic and construction games. He enjoys recreational activities, particularly playing ball, searching for elements, and visiting parks or rivers. He enjoys fruits such as bananas, watermelon, tangerines, and oranges. He dislikes pineapple and chopped papaya (though he accepts papaya in juice form). He benefits from a structured sleep routine, sleeping easily and restfully, which contributes positively to his mood and willingness to participate in daily activities.

Yoshi requires a parenting style that combines deep affection with structure. His ideal home will prioritize his medical and therapeutic needs—including ongoing nutritional support and developmental therapies—while providing an emotionally safe and orderly environment.

Gannon #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Listed: Sep 2025

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Other mixed disorders of behavior and emotions. Disorder in psychological development, unspecified. Moderate cognitive delay, without mention of behavioral disorder

Joshua #

Boy, Age: 4

Primary Diagnosis: Blind / VI, Cerebral palsy, Global developmental delays, Hydrocephalus

Listed: Sep 2025

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Congenital anomaly of the central nervous system – hydrocephalus; condition after implantation of a ventriculo-peritoneal shunt. Epilepsy. Bronchopulmonary dysplasia. Non-allergic asthma. Cortical blindness. Spastic quadriparesis. Severe developmental delay. Atopic dermatitis.

Lexi

Girl, Age: 4

Country Code: LA-6

Region: Latin America

Primary Diagnosis: Deaf / HoH

Listed: Sep 2025

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Lexi is a bright-eyed 4-year-old girl with bilateral hearing loss and developmental delays, but these do not diminish her joyful spirit. Lexi communicates in her own unique ways and is curious about the world around her. Lexi will thrive in an environment where she receives consistent, patient attention and where her efforts to communicate are celebrated. She’s looking for a family who will provide a nurturing and stimulating home, eager to support her continued development and help her reach new milestones. With love and encouragement, Lexi has the potential to blossom and bring immense joy to her adoptive family.

Arlen

Boy, Age: 10

Country Code: LA-2

Region: Latin America

Primary Diagnosis: ADHD, Epilepsy/ seizure disorder, Other Special Needs

Listed: Jul 2025

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Arlen and his four siblings came into care in 2022 due to being victims of multiple types of abuse in their family. Their parents were known to be drug users with emotional instability and aggressive behaviors between them. They were also verbally abusive toward the police and other authorities. Arlen is being placed for adoption as a single child.

As Arlen was never enrolled in school until he was taken into protective custody, he is in the first grade. He is familiar with some letters and numbers but cannot read or do simple arithmetic problems. He truly enjoys art class since he has great skills for doing crafts. He seeks adult validation in every activity he participates in. However, while he recognizes authority figures, he is defiant toward them and only obeys with some difficulty. Arlen usually gets along well with peers and adults; however, when he gets mad or frustrated, he begins to behave in a bad and aggressive way. He lies whenever he wants to avoid his responsibilities. He gets upset when he cannot do what he wants. His cognitive development is affected. Arlen has been diagnosed with ADHD, mild cognitive developmental delay, focalized epilepsy, and oppositional defiant disorder. He goes to occupational and psychiatric therapy, and also takes daily medication. There are no concerns regarding his motor and language development.

As mentioned, Arlen and his siblings were subjected to multiple types of abuse. It has been reported by his teachers that in addition to being aggressive toward other children in the class. Though Arlen can verbally express his feelings and emotions, he has a hard time managing them. He gets easily frustrated and has trouble finishing any given task. He is afraid of the dark and of being alone. Arlen gets anxious when he consumes sugary foods, and he also gets anxious when an outing is going to happen soon. He goes to bed around 8 pm but takes a long time to fall asleep.

Even though Arlen has been known to be aggressive toward others, his child study also reports he usually gets along with adults, peers, younger children and animals. Arlen is not shy when meeting people; it is easy for him to take the initiative to start a conversation with anybody. He likes to take the lead in any game. Arlen can be affectionate toward those he knows and is comfortable with. He likes to maintain good hygiene habits and takes care of his personal belongings.

Arlen is very active during the day. He loves to go to the park and to play soccer with friends. Arlen is interested in any outdoor recreational activity; he loves to do physical exercise. He has stated that he is good at swimming. Arlen has stated that he would love to get married and have kids. He does not want to go to college but would like to work handling heavy machines. He is open to being adopted by any type of family.

Kalin

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Autism, Blind / VI

autism, asthma, congenital cataracts, and overall developmental delay

Listed: Apr 2025

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Date of the report: 7/3/2024

Kalin came into care as a baby when his mother brought him to the hospital and it was discovered he was in poor condition. He had a high fever, was malnourished, had a diaper rash and was noted to have overall developmental delay as well as cataracts. His mother was an older teenager and she had not sought any care for the medical condition he had had at birth. Kalin was 5 years, 8 months old at the time of this report from July 2024. Kalin´s current diagnoses are autism, unspecified asthma, congenital cataracts, and overall developmental delay. He takes daily medication. Kalin still wears diapers during the day and night.

Kalin is not formally enrolled in school. He has been diagnosed with autism and unspecified overall developmental delay. He currently goes to physical, occupational, speech, and psychological therapy. The psychiatrist recommended the foster mother take the child to school gradually. He goes to pre-k two days a week and for just a couple of hours. At first, he did not want to stay there but over time, the foster mother states that he is used to going to school and enjoys his time there. He loves toys that make different sounds, and he can play alone for more than 15 minutes.

There are no major concerns regarding Kalin´s gross motor skills, and he is still improving his fine motor skills. Since he is now used to wearing his glasses, this has helped him with his sense of feeling safe to perform different physical activities. He is starting to talk with some difficulties; however, through sounds and facial gestures, it is easy to understand what he wants. He has begun to imitate the sounds of some animals. Kalin is able to identify people´s emotions by looking at their facial expressions. He is able to give and receive affection with those he is familiar with, and he does not get jealous when his caregiver pays attention to other children. He is not shy—whenever he arrives at a new place, he explores his surroundings interacting with adults or kids. At times, Kalin gets anxious when he wants to play with something but needs to wait. Sometimes he gets upset when he is hungry and his food is not ready or he needs to wait for it to cool down. He is afraid of sudden loud noises.

Kalin enjoys playing with toys that make music. The child´s favorite food is spaghetti with chicken or ground beef. He is interested in musical instruments.

Clyde

Boy, Age: 14

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Down syndrome

Down syndrome; Cognitive delays; Sleep apnea; Hypothryoidism

Listed: Apr 2025

*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Clyde attends school three times a week and works with guides at home on the other two days. He has a cooperative attitude when it comes to his schooling. He has greatly improved in carrying out certain activities semi-independently, such as making his bed with supervision, choosing clothes, feeding himself, going to the bathroom, and picking up his room. In his free time, Clyde attends crochet classes 3 days a week for an hour, which consists of making dolls. Clyde loves to watch cartoons. He would thrive in a family that can maintain a structured and predictable routine to provide security and emotional stability. Contact the agency to learn more about Clyde and his listed needs!

The agency has several videos available, too!

Alex

Boy, Age: 14

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Older Child, Trauma History

Listed: Mar 2025

**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Information in this report is from January 2023 when Alex was 11. The agency can attempt to get updated information if they receive a serious inquiry.

Alex is a clinically healthy 13-year-old boy who came into care in mid-2021 with his older sister, but she escaped the facility and her whereabouts are unknown. Alex does not have any cognitive, emotional, social, physical or other known conditions (as of his last report). He is developing in an age-appropriate manner. However, Alex has been receiving psychological services to help him work through the loss of his mother and sister as well as recover from reported abuse. His therapy has successfully helped him develop coping strategies for when he is feeling anxious, sad or just needs guidance.

When Alex came into care, he was 10 years old but did not know how to read, write or perform basic math However, he was enrolled in school in the third grade and even in the short time he has been in school (as of this report when he was 11) he is already reading, writing, and doing math on a third grade level. He actually was being promoted to the sixth grade to help him be more on the level of students his age. He shows an interest in the area of learning religion. He and his foster family attend a Christian church, which he enjoys. He also participates in theater classes and soccer at school. He is respective of authority figures and gets along well with his peers.

Alex enjoys outdoor activities such as soccer, cycling and skateboarding in addition to his theater classes. He especially loves family activities such as birthdays and holidays. While Alex enjoys participating in family activities with his foster family, he sometimes becomes anxious during these outings. When this happens, he is able to cope with his anxiety with the help of his foster mother. His foster parents are also helping him to build patience and learning to be punctual, which is an area he struggles in. Alex experiences moments of sadness when he thinks about his biological family, but he has learned to cope with these times with the help of his foster family and through methods learned in therapy. He is afraid of the dark and tries to go to sleep quickly to help manage this fear. Alex has developed a tolerance for the frustration he feels and demonstrates a mature understanding of others’ strengths and weaknesses.

Alex is a resilient, emotionally stable, and healthy child. He has made significant progress through difficult life circumstances, showing a readiness to continue his growth in a supportive family environment. His psychosocial team has been talking to him about adoption and he expresses an openness to being adopted with a preference for heterosexual parents, whether a couple or single parent. His openness to adoption and capacity for adaptation suggest he is prepared for a bright future.

West

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Cerebral palsy, Global developmental delays

Cerebral Palsy, full paralysis; Severe cognitive delay

Listed: Mar 2025

2025 MACC, Available to Large Families, Available to Single Fathers, Available to Single Mothers

West is a calm and precious boy who reacts with his eyes when he hears the voices of his caregivers who he adores. He loves to have his face caressed. West will fix his gaze on those he loves dearly. He receives therapies twice a day. Loud noises tend to startle him. West enjoys a calm and peaceful environment. He is beloved amongst all the staff. There is more to West’s gaze than meets the eye; in his eyes is a desire to be wanted. Would you give West the chance to be loved and make those eyes come to life?

VIDEO:
https://vimeo.com/manage/videos/1065191610
Password: Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances (with a specific adoption agency).

Idris #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Global developmental delays

Cerebral Palsy – spastic quadriparesis. Localized (focal, partial) symptomatic epilepsy and epileptic syndromes with complex partial convulsions. Severe mental retardation, significant behavioral disorders requiring care or treatment. Optic nerve atrophy.

Listed: Mar 2025

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Idris was born with very low weight and immaturity, complicated neonatal period. Subsequently, with the development of multicystic encephalopathy with microcephaly (based on severe hypoxic-ischemic incidents in the perinatal period), severe spastic quadriparesis and symptomatic epilepsy (mainly tonic seizures). Conducts therapy with Convulex, as a result of which seizures are almost not registered.

The child has severe lag in physical and neuropsychiatric development. Severe mental deficiency. Needs systematic motor rehabilitation, classes with a speech therapist, psychologist and typhlopedagogue. Weak rehabilitation potential. Followed by a pediatric neurologist and ophthalmologist.

The child can turn from back to stomach and back. Does not crawl, does not sit independently, does not have a four-legged stand. Does not stand up, holding on to a support. Holds a toy placed in the hand for a short time. Lacks a pincer grip. The average mental age of the child corresponds to 3-5 months. The child is mostly calm with accompanying episodes of irritability, expressed through crying. Quickly calms down by the presence and attention of an adult. There are no indications of aggressive behavior or manifestations. Does not utter words, syllables and sound imitations. Does not turn when called by name. Does not initiate contact with other children. The child is completely dependent on the care of an adult. Takes food from an adult with a spoon (less often from a bottle). Falls asleep independently.

There is evidence of a brother with an autoimmune disease – Alopecia areata.

Malachi #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Posthemorrhagic extreme internal hydrocephalus; implantation of a ventriculoperitoneal shunt (VPS). Bronchopulmonary dysplasia. Retinopathy of prematurity

Listed: Feb 2025

2025 MACC, 25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

He lives in a home for medical and social childcare. He was born to a minor mother who had epilepsy and took anti-epileptic medications during pregnancy. There was a complicated pregnancy and birth, resulting in extreme posthemorrhagic hydrocephalus. A shunt was implanted but failed. A new one was inserted. Malachi is on permanent antiepileptic monotherapy, without convulsive manifestations.

Due to the extreme hydrocephalus, Malachi is in impaired general condition, with significant lag in psychomotor development – no head control, does not turn around, does not sit or stand. He needs specialized care, monitoring by medical specialists, and daily medical rehabilitation. He is usually in a positive emotional state. He coos frequently and continuously. He reacts animatedly to the speech of an adult. He initiates a desire for physical contact by smiling. The boy is completely dependent on the care of an adult. His sleep is peaceful. He takes food with a pacifier. The agency has videos of him.

Theodore #

Boy, Age: 8

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Deaf / HoH, Hydrocephalus

Listed: Jan 2025

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Internal obstructive hydrocephalus – VPA. Spastic cerebral palsy. Umbilical hernia. Convergent strabismus. Hemangioma pedis dextra. ROP in regress. Bilateral sensorineural hearing loss – hearing aid. Mixed specific disorders of psychological development. Severe mental delays.

Shane #

Boy, Age: 16

Region: Eastern Europe

Primary Diagnosis: Behavior, Learning Disability

Listed: Jan 2025

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

A male child with age-appropriate physical and neuropsychic development. Attended irregular school, with unlearned elementary school skills and knowledge. With aggressive manifestations upon minor provocations. Intellectual level – borderline low IQ.

Paul #

Boy, Age: 2

Region: Eastern Europe

Primary Diagnosis: Blind / VI

Iris coloboma

Listed: Jan 2025

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Paul can crawl, pull to a stand, walk holding the hand of an adult and has recently started taking steps independently. He knows where his toys are kept in the house (toy boxes) and will go to them to get his toys. His fine motor skills are well developed. He transfers small objects from hand to hand and has a pincer grasp. He shows an interest in toys and outdoor activities, such as swinging. He enjoys cause and effect toys. His speech is starting to develop. He “babbles”, saying syllables such as “da-da” and “ba-ba”. He is attached to familiar people and expresses his emotions in age appropriate ways. He was recently prescribed glasses to help with his vision issues.

Adam & Vinny #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Autism

Delays, Autism

Listed: Jan 2025

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, Siblings

The boys lived with their birth family until they were 22 months old. They were removed from the birth family and placed in foster care at that time.

Adam has been diagnosed with an intellectual delay, but he continues to make progress in all aspects of his development and learn new skills. His gross motor skills are developmentally appropriate for his age. He can walk, run, climb, etc. His fine motor skills are slightly delayed. He nests nesting boards according to the principle trial and error. He can build a tower with 10 blocks. He can draw a circle but he can’t draw an emoticon. He can string and sort small figures. He cuts with scissors, forms worms out of playdoh and cuts them. He currently cannot copy shapes and letters according to a pattern. His attention span when working on tasks continues to increase. He has a well-developed visual memory. He will imitate gestures and movements. He can group objects by color and shape, but cannot currently identify colors and shapes by name. He understands what is said to him and can follow one step directions. He has pretend play skills. He can easily navigate in familiar environments. His speech is still developing. He can say some simple words and attempts to communicate using gestures. He is currently attending preschool, and has adjusted well to this environment. He participates in group activities and plays with the other children. He enjoys playing with playdough and participating in music and games. He helps clean up after activities. His self-help skills are developing. He is toilet trained. He is working with specialists to continue to develop his skills.

Vinny has been diagnosed with childhood Autism, but continues to make progress and learn new skills. He can walk, run, climb, throw and kick a ball. He can build a tower with 10 cubes, he strings and sorts small figures. He cuts with scissors and he tries to cut along a drawn line. He has difficulties doing puzzles. He has difficulty concentrating during certain tasks. He is more focused and attentive during activities related to language educational games and modelling with playdoh. He has a strongly pronounced mechanical memory. He has difficulties making the relation between a symbol and a word. He compares objects by color and shape but does not recognize or name them. He understands single-step commands. He participates in role games (he puts a doll to bed and tucks her in). When he sees pictures with objects from everyday life (a broom, glass, spoon) he shows the activities that he performs with them. His speech is delayed (he says very few words), but he attempts to communicate using gestures. He demonstrates attachment to his caregivers and gets along with other children at preschool. He enjoys playing with playdough and educational cards. His self-help skills are developing. He is toilet trained. He is working with specialists to continue to develop his skills.

Owyn #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Listed: Jan 2025

2025 MACC, 25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Precious Owyn is looking for a special family.

He is diagnosed with hydrocephalus and has some other medical issues that require in-depth care. The adoption agency has a lot more photos and more information about his needs and video footage. A specific adoption agency also has grant funding in the amount of $2500 available.

Jordy and Mike #

Sibling Group

Ages: 13, 15

Region: Eastern Europe

Primary Diagnosis: Older Child

Listed: Jan 2025

**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, Siblings

Jordy and Mike are ready for a family. Agency staff who met them said, “they are clinically healthy and very well behaved and raised children. They are doing great at school on many subjects which is rare in general for abandoned children. The fact that they have been raised in foster care by a nice family, is definitely helping them.”

Please consider bringing these boys into your family for the New Year. The agency has a lot more photos and information and videos to see these great boys! A specific adoption agency has grant funding in the amount of $2500 available.

Morty #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder

grand mal seizures

Listed: Jan 2025

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Morty is looking for a very loving family who has time to spend helping with his needs. He has been diagnosed with grand mal seizures and takes medication for this. He has other delays in all aspects of his development. The agency has video available, for inquiring families.

Maren & Aiden #

Sibling Group

Ages: 17, 13

Region: Eastern Europe

Primary Diagnosis: Older Child

Listed: Jan 2025

**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, Siblings

MAREN: Clinically healthy

AIDEN: Clinically healthy

Sophie

Girl, Age: 10

Country Code: Asia.4

Region: Asia

Primary Diagnosis: Cerebral palsy, Other Special Needs

Listed: Dec 2024

Available to Single Fathers, Available to Single Mothers

Sophie is a gentle, cheerful, and agreeable 8-year-old girl. She loves listening to music and is attracted to various sensory toys and materials. When her caregivers and teachers play music, she becomes attentive and smiles. Sophie has been diagnosed with cerebral palsy with multiple medical conditions. She requires daily medications and intensive medical follow-up in various specialties. She needs support and assistance with mobility and daily living activities. In the face of her challenges, Sophie works hard to participate in different training sessions and therapies including physiotherapy and occupational therapy.

Sophie loves people. She can be easily comforted by hugging, gentle stroke, and comforting words. Sophie expresses herself nonverbally. She nods or smiles when she likes something, and pouts or frowns when she does not. She joyously participates in the activities the caregivers and teachers give her such as sunbathing outside and sensory activities. Her caregivers and teachers report that she is easy to care for and manage because of her calm nature and generally stable health condition. She also adjusts to changes quickly and easily.

It is believed Sophie will continue to make progress in reaching her potential within a loving and caring family. Due to the unique child/family matching system in her country, a family with a current home study for any country can submit to be considered to become her family.

Kyle #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Microcephaly. External hydrocephalus. Delay in neuropsychological development. Moderate mental delays. Suspicion for Seckel’s syndrome

Listed: Dec 2024

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Kenny #

Boy, Age: 9

Region: Eastern Europe

moderate mental delay, behavioral issues

Listed: Dec 2024

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Hans

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Epilepsy/ seizure disorder, Hydrocephalus

Hydrocephalus; Epilepsy; Cerebral palsy; Macrocephaly, hip dislocation; gastrostomy

Listed: Nov 2024

25 for 2025, Available to Large Families, Available to Single Fathers, Available to Single Mothers

Information in this report is from November 2024

Hans was born to a young teenage girl who, tragically, had already given birth to a child at a very young age. Due to her chronological age and emotional immaturity the mother was not able to fully understand her responsibility, and despite the support of her family, the bond between Hans and his mother was not positive. After Protection Services became involved, it was evident that the biological mother and her family were not able to take care of the child due to his special needs, economic struggles and already caring for Hans’s older sibling. He, therefore, came into care at the age of 3 years old. There is no information about the biological father.

Hans is not enrolled in school due to his medical diagnoses. Hans loves to receive affection, and he responds through smiles. He is totally dependent on others to fulfill his daily routines. He communicates through guttural sounds, screams or by crying. Hans cries whenever his diaper is dirty. Hans´s gross and fine motor skills are not developed. The child cannot hold his head up, and he cannot crawl or walk. He has some body movements, and the foster mother has received training on how to stimulate his motor development. He does not like to be held and prefers when people change his body position without holding him for too long. Due to Hans’s medical diagnosis, he has a severe cognitive delay and is not able to interact with other children. Hans receives occupational, physical and speech therapy. Hans takes daily medication.

Hans likes to listen to soft music. He needs a family who can always take care of him due to the severity of his condition.

Dezi

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Epilepsy/ seizure disorder, Genetic Condition (non-DS)

severe mental delay, significant behavioral disorders, overall developmental delay, overall developmental disorder, epilepsy, Soto Syndrome

Listed: Oct 2024

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Information in this report is from July 2024:

Dezi lived with his biological parents and older sibling until he was almost four years old. While his parents tried to take care of him, money was always lacking and ultimately, his parents knew they could not meet Dezi’s healthcare needs. In order for him to get all the help he needs and to have a better life, his parents relinquished him to protective care services in July 2022.

Due to the child´s medical diagnosis, he is not enrolled in school. There were two times were Dezi attended a special school, but his needs were much greater than what the teachers could manage. Dezi´s adjustment to a foster home was challenging but his current foster mother has done a great job with him. He has developed a strong bond with his foster mother and regulates his emotions in accordance with what she is doing or how close she is to him. He is now able to give and receive affection, which is a great achievement, and he even sometimes gets jealous when his foster mother pays attention to the other children. Dezi’s language is almost nonexistent, but he says a few words such as “ma.” He communicates mostly through facial gestures and by pointing at things he wants to grab or do. When Dezi gets upset, he cries and has “tantrums,” throws objects, and lays himself on the floor. Dezi is not comfortable being around people he is not familiar with. If he likes somebody, he will usually pull that person by the arm to start a game. Dezi likes to play with other children for short periods, and he is not aggressive towards them. He gets anxious when he is not familiar with an environment. He gets upset when he is not allowed to do something or eat at different moments throughout the day.

Dezi is very active, he changes from one activity to another in short periods, it is very hard for him to focus his attention on one specific thing. There are no concerns regarding his gross motor development, he is still working on his fine motor skills. He needs guidance and support to fulfill his daily routines though there are some activities that he can do on his own, such as eating with no help and dressing up. He sleeps throughout the night without any inconvenience. Dezi does not wear diapers during the day as he can go to the bathroom alone but needs help to clean himself up; he wears diapers during the night. He does not like animals.

Dezi’s favorite show is Paw Patrol. He gets happy when he gets new toys, especially cars even though toys do not usually last a long time because he plays roughly with them. He likes to wear clothes with Superman logos or drawings. Dezi has a good appetite and eats every kind of food. He likes to play with water.

Evan and Michael

Sibling Group

Ages: 14, 16

Region: Eastern Europe

Primary Diagnosis: Older Child

Listed: Oct 2024

**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

EVAN — Diagnosis: clinically healthy

MICHAEL — Diagnosis: clinically healthy IQ71

Everett #

Boy, Age: 15

Region: Eastern Europe

Primary Diagnosis: Autism

autism and severe delays in intellectual functioning; non-verbal

Listed: Oct 2024

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Everett resides in a center for children. He is a healthy, good-looking boy who has autism with severe delays in intellectual functioning. He makes sounds but has no speech skills. He shows stereotypical mannerisms of rocking, hand fluttering, and hyperactivity. He plays by himself and does not interact with others. He seldom reacts to his name. Sometimes he self-harms or shows frustration. He does not sustain attention for very long. He needs assistance in feeding, clothing and self-care. He needs close attention. He needs a loving family.

Videos are available.

Mell

Boy, Age: 4

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Hydrocephalus, Spina bifida

bilateral hip dysplasia with congenital hip dislocation, congenital hydrocephalus, lumbosacral meningocele corrected, congenital malformation of the corpus callosum, hypermetropy (far-sightedness), and malnutrition.

Listed: Oct 2024

25 for 2025, Available to Large Families, Available to Single Fathers, Available to Single Mothers

Info from March 2024:

When Mell was born, his biological parents tried to take care of him even with his special needs, but they lived in a small town far away from cities and hospitals. At his one month check-up, he was diagnosed with congenital malformation of the spinal cord, hydrocephalus, low weight, fetal growth delay, and respiratory syndrome. At one of his following check-ups, the doctor sent Mell to the hospital due to a high fever and inflammation of the brain. Sadly, though they had tried, his parents recognized that they did not have the means of caring for him in the ways he needed, both due to finances and distance from necessary medical care, and they asked Protective Services to care for him. No other family members were able to provide the care he needed as well. Mell was placed in a foster home and is doing well.

Mell has been receiving various types of therapies which have been valuable in his development. When meeting adults for the first time, he becomes shy, but he recognizes familiar people and loves to interact with them. Mell identifies the emotions on people´s faces and interacts accordingly. He is a very expressive child who shows affection in various ways, and sometimes gets jealous when his foster mother gives affection to the other children. According to the professionals who care for him, Mell has the language development of a 12-month toddler. He communicates through crying and screaming and can say some short words such as “mama” and “papa.” He also imitates animal sounds, such as those of a dog or cat. He responds to simple instructions such “Take this” and “Give me that.” Mell identifies different body parts, plays with Play-Dough, and performs other activities that strengthen his fine motor skills. His movements are spontaneous despite the limitations he has in his lower limbs. Due to his chronological age, Mell requires support, supervision, and guidance to fulfill his daily routines. Mell takes two naps during the day and sleeps throughout the night. He wears diapers all day.

Mell likes to interact with peers or adults and loves to spend time outside. He gets excited when he hears a motorcycle engine as he immediately thinks he is going to go out and gets anxious. He gets upset when his diaper is dirty and when he is not allowed to go out. Mell gets happy with simple things, and he likes to laugh a lot. Mell loves to drink sweet juices. Due to his medical condition, he does not wear shoes but wears very soft socks. He enjoys it when adults help him to kick the ball to play soccer. Mell also likes to play with cars and airplanes.

Lilian and Sonny

Sibling Group

Ages: 10, 7

Country Code: LA-7

Region: Latin America

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder

Sonny is a quadriplegic child with cerebral palsy and epilepsy.

Listed: Oct 2024

2025 MACC, Available to Single Fathers, Available to Single Mothers, Siblings

Lilian is described as happy and communicative girl who is very creative. She interacts positively with adults and other children. She is currently in the fifth grade where she is known to be a good student.

Sonny is a quiet boy though he smiles and babbles to communicate with others. He is a quadriplegic child with cerebral palsy and epilepsy.

The agency can attempt to obtain additional information for interested families.

Declan

Boy, Age: 9

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Down syndrome

Down syndrome

Listed: Oct 2024

*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Our sweet Delcan, was born in May of 2017 with Down Syndrome. We are so excited to share his referral with interested families.

There is a $1,000 agency fee reduction for Declan’s adoption with a specific agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-declan10
https://vimeo.com/maaspecialkids/maa-declan11

Password: Adoptmaa

Kevin #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus, Spina bifida

Congenital anomaly of the nervous system: internal hydrocephaly; condition after ventriculo-peritoneal anastomosis implantation. Holoprosencephaly. Lumbosacral spina bifida aperta; condition after plastic surgery. Lower flaccid paraplegia. Pelvic-reservoir incontinence. Delayed neuro-psychic development

Listed: Sep 2024

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Kevin can sit on his own. He plays with toys. He interacts positively with caregivers. He makes some sounds, but is not yet saying any words.

Nate

Boy, Age: 6

Country Code: LA-7

Region: Latin America

Primary Diagnosis: Cerebral palsy

Premature birth, Cerebral palsy

Listed: Sep 2024

25 for 2025, Available to Single Fathers, Available to Single Mothers

Information in this report is from Summer 2024:

Nate was born prematurely at 27 weeks gestation and was hospitalized for two months. After living with his mother for two months, he came into protective care at 4 months old after his mother abandoned him in the care of a neighbor. Initially she visited him occasionally, but the last visit was in 2022. Nate lives with a foster family.

Nate has unidentified cerebral palsy, but it doesn’t hold him down! While at 8- months-old he showed significant delays in neuro-psychomotor development, today he has shown significant development. He is being monitored a team of specialists including a neuro-pediatrician, orthopedist, physiotherapist, psychologist, speech therapist and nutritionist, in addition to receiving specialized educational care. Nate can now move around with some independence and is in the process of adapting to the use of an orthotic equipment, which may help his locomotion. According to the physiotherapist’s report, Natey crawls, sits in a W position with balance, stands with support and walks sideways. He has the potential to use a walker for home distances and a wheelchair for community distances.

Socially, Nate is an extroverted child who loves to participate in activities and communicate. He can focus on activities. He understands what is asked of him and responds coherently within his ability. He demonstrates caring and affection with other children and adults. He is observant to what is going on around him. Nate lives in a house where there are children younger than him and this fact limits his social interactions, which has significantly compromised his progress.

It is believed that Nate has great potential for development, as long as there is proper stimulation. The possibility of starting family life through adoption at this time is considered extremely important for the progress of the child’s physical, social and cognitive development.

Dillon

Boy, Age: 12

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Autism

academic skills disorders, hyperactivity and attention deficit disorder, autism, hypotonia, expressive language disorder, speech and language developmental delay, mild mental delay, and behavioral disorders. He takes daily medication.

Listed: Aug 2024

Available to Large Families, Available to Single Fathers

Dillon, 10, entered protective care he was 16 months old due to his mother’s inability to care for him. The grandmother indicated that his mother had mental health issues, but that she had been unable to get her to seek psychiatric care.

Dillon is in the 2nd grade. He is respectful towards his teacher and classmates. It is hard for him to fully understand subjects such as math and language, but improvements have been made in his reading. According to an IQ test, his intelligence is lower than expected for his age. He can stay focused for short periods.

Dillon´s social development has been challenging. During the pandemic he did not interact with other children. He is currently learning to be calm during his interactions and not to become aggressive towards them. Dillon participates in group activities for short periods since he might become aggressive or behave in a bad way. There are days when a situation has triggered Dillon and he then does not want to obey instructions. Dillon gets anxious about loud noises and insects. Sometimes Dillon demands the full attention of his foster mother. While Dillon is very affectionate towards people he is familiar with, he gets anxious and nervous when around unfamiliar people. He gets worried about going out, mainly because he worries about unknown people. Dillon is still learning to manage his impulses and frustrations, and when he is upset he usually hits the walls and screams. It is important to mention that Dillon gets along better with younger children than with his peers. Dillon’s fine psychomotor skills have improved over time. There are no major concerns regarding his gross motor skills; however, due to his diagnosis, he is restless and harms himself sometimes. Dillon is learning to become independent in his daily routines, but he still needs supervision and support. He has good sleep and eating habits. Dillon is still learning to urinary and bowel control, and he often will urinate/defecate outside instead of going to the restroom. He does not take care of his personal belongings and is still learning to have proper hygiene habits.

Going to the park or getting to do errands with his foster mother makes Dillon happy. He likes to play alone, and he has a favorite outfit that he would love to wear every single day.

Bowie #

Boy, Age: 8

Region: Eastern Europe

Primary Diagnosis: Blind / VI, Cerebral palsy, Epilepsy/ seizure disorder

Vision issues, cerebral palsy, seizures

Listed: Sep 2024

25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Please meet this cute boy named Bowie. He was diagnosed with congenital cataracts in both eyes. However he underwent surgical treatment with implantation of intraocular lenses. There is suspected Glaucoma. He is also diagnosed with Children’s cerebral palsy – Quadri pyramidal syndrome. Grand mal seizures with or without petit mal seizures.

Bowie can sit up independently from a lying position. He can stand up by holding on to various objects. He walks independently but it is uncoordinated. The child lags in neuropsychological development. He accepts bodily closeness with pleasure. It is pleasant for him to be held by an adult. The presence of children in his immediate space does not bother him, but he does not show interest in them and does not initiate interaction. He is soothed by riding in a pram or listening to favorite children’s songs. He prefers the environment to be quiet. He becomes nervous and anxious around loud noise. He is entirely dependent on the care of an adult.

Brandon #

Boy, Age: 6

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Hydrocephalus

Microcephaly. Hydrocephalus. Agenesis of the left hemisphere, persistent foramen ovale, Interatrial defect and Schizencephaly.

Listed: Sep 2024

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Please meet Brandon; he has multiple special needs. Sadly Brandon relies totally on the care of others. He sleeps in a room with four other children. The caretaker says he seems to like music and likes the bath. He can make some sounds for speech. He has difficulty feeding and swallowing.

The agency staff member that met Brandon said the following: “According to the caretaker, there is a slight regression, especially in terms of feeding. Unfortunately, I have not been given an opportunity to speak to any of the specialists engaged with the boy and possibly what exactly they are working on. Brandon could have some potential, but it’s very hard to tell. In any case, he needs a lot of love, a lot of attention and a lot of activities.” Could you be the family for Brandon?

Pah

Boy, Age: 5

Country Code: Asia.4

Region: Asia

Primary Diagnosis: Autism, Global developmental delays

Listed: Sep 2024

Available to Single Fathers, Available to Single Mothers

Pah is a lovely little 4-year-old boy in need of a permanent home. He has been with his foster family since he a little baby. He is bonded to his foster family as well as another foster child in the home who is 3 months younger than him.

Pah currently is in good normal health. However, when Pah was 22 days old he showed peripheral pulmonary artery stenosis, small patent foramen ovale (PFO), and secundum atrial septic defect 1.5 mm. On the follow-up echocardiogram in April 2022, the results showed normal heart anatomy and function. As of his August 2024 child checkup, his hearing and vision were reported to be normal. While Pah’s physical health remains good, he has been diagnosed with Autism Spectrum Disorder (ASD) in August 2023, for which he attends Child and Adolescent Psychiatry therapy. During the same evaluation, he was assessed to have a mild delay in gross motor skills as well as a mild delay in oral language. He had been previously diagnosed in 2022 with Borderline Developmental Delay. As observed, he can speak clearly, except that he may mispronounce some words. He is able to hold conversations with adults and express his needs and feelings in sentences. He can also follow instructions. Pah receives speech therapy about 2 times per month, and physiotherapy and occupational therapy 3-4 times per year at school. Pah can walk and run confidently. He can jump forward 12inches with both feet, stand on one leg, walk upstairs and downstairs with alternative feet by holding onto the handrail, throw and catch a ball, and kick a ball forward 5 feet away. He can also climb up the rope net. In terms of fine motor skills, Pah can build a tower of 9 blocks, remove bottle caps, hold a pen to draw, turn pages one by one, and thread beads.

Pah is described as a happy, outgoing but also stubborn child who has shown improvements in his emotional expression. He has become more accepting of reasoning as he gets older. Due to his ASD features, Pah has a set way of doing things. He also tends to cry easily over trivial things such as when he cannot find a toy or complete a task on his own. Pah shares a normal relationship with the other foster child in the home. They have typical sibling-like rivalries and will sometimes fight over toys. He shares a close relationship with the foster mother and accepts her guidance and follows her instructions. Overall, Pah is generally an easy child to take care of. He is well-behaved and manageable most of the time except that he tends to cry easily and can also be quite stubborn at times.

Pah performs well in his self-care tasks. Being able to drink from a cup and a straw, he can feed himself with spoon and a fork. He can wash and dry his hands with a towel; put on and take off his clothes, shoes and socks; brush his teeth and wash his face. He has finished toilet training and does not need to wear diapers. He can go to the toilet by himself. He only needs assistance in bathing, washing his hair and cleaning after a bowel movement.

Pah is attending pre-kindergarten at a nursery school. As described by the teacher, Pah has some close friends at school and enjoys a satisfactory relationship with his teachers. He can follow school rules and routines. Being attentive in class, he enjoys participating indifferent activities. As described, Pah is sometimes sensitive to the teacher’s reminders and sometimes is emotional about this. Pah knows lots of colors, shapes, fruits, animals, food and body parts. He also knows some concepts such as “big-small,” “up-down,” etc. He can recite the numbers from 1 to 50 and recognize some letters and numbers. He can tell others his name and age.

Families with a home study prepared for any international country can submit for consideration of Pah. The agency program specialist can explain the child/family matching process in his country.

Samson #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Global developmental delays, Hydrocephalus, Spina bifida

hydrocephalus, spina bifida in the lumbosacral area –condition following implantation of a VP shunt and closing of the spinal defect; lower flaccid paraplegia; pelvic reservoir incontinence; delayed psychomotor development; delayed psychological development.

Listed: Aug 2024

2025 MACC, 25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Sizable Grants $5,000+

Update Nov 2024: Samson was recently moved from a large orphanage to a small group home for children with disabilities. He loves attention and responds with joy with staff interacts with him. He is described as a calm and radiant child.

Samson sits independently and can stay in this position for extended period of time. He reaches for distant toys by directing his hands and turning his torso towards the desired direction and after that he pulls the toy. He prefers toys with buttons, which make sounds, light or melody, as well as toys with movable elements, which he can spin. He initiates interactions with adults, whom he likes and with children. Samson enjoys being praised and reacts with discontent when something is being denied or forbidden to him. He is fed via baby bottle and spoon.

Salazar #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Global developmental delays, Speech Delay

Mild to moderate mental delay. Delay in expressive speech. Hyperopia. Astigmatism.
Intermittent heterotropy. Low birth weight, moderate mental delays

Listed: Aug 2024

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Salvador has resided with a foster family since July 2018.

He was born with low weight and with pathological neonatal period. The child has a
physical development within the lower limit of the norm and mental delay in mild to moderate degree (IQ-41). Phrase speech is not developed, he utters single words; lags behind in the development of habits, skills, emotional and social development.
Uses optical correction due to intermittent heterotropy and astigmatism of the eyes.

The child walks stably and independently. There is delay in the development of the fine motor skills. The emotional status of the child is mostly positive – he is calm and curious. He does not show aggression, he is adaptive. He understands phrasal speech, utters single words, but does not speak. The child is able to play by himself, but he also is looking for the company of other children. Participates in the game process. He feeds himself, his personal hygiene is well-maintained. He controls physiological needs.

Roman

Boy, Age: 13

Country Code: LA-2

Region: Latin America

anxiety disorder; unspecified emotional and behavioral disorder

Listed: Aug 2024

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Single Fathers, Available to Single Mothers

Report is from August 2024 — Roman, 12, lived with his biological and an older brother until he was 7 years old. At that time, the place where his mother worked burned and she had to leave his brother with that child’s father, and she moved to a different town with Roman. Unfortunately, she could not find a stable job or place to live and she sought assistance from Protective Services. Roman was previously hosted by a family, but that family opted not to adopt him. More information is available.

Roman is in the 4th grade. It has been observed that Roman has great leadership skills, especially at school. Most of his teachers have stated that Roman has a lot of potential but his lack of motivation hinders his progress and development. However, Roman has great skills in math. He recognizes authority figures; he is respectful and obedient towards them. He can follow simple and complex instructions. There are no concerns regarding his motor, language, cognitive and social development.

Roman is an affectionate child after he has built a positive relationship with an adult. He can verbally express his feelings and emotions; however, when there are situations of high emotional demand, he limits the externalization of what he is feeling. Roman is still learning to manage his frustration and impulses, but good improvements have been observed. Roman is shy when meeting people but can easily overcome this behavior once he feels the adult is trustworthy. He interacts in a positive way with adults, peers, younger children, and animals. Roman gets anxious when he does not get what he wants immediately or when something he was expecting does not end up happening. Roman is sad when remembering his biological family, and this connection is part of why the hosting family did not choose to adopt him. Roman is afraid of dark, thunder, rain, and heights. In order to fall asleep, he needs some light or a stuffed animal.

Roman loves it when he gets to go to amusement parks, the movies or the pool. Roman likes to ride his bike, listen to music, and watch TV. He has stated that he would like to improve his drawing skills.

Jaxon

Boy, Age: 9

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Deaf / HoH, Down syndrome

Down syndrome; Bilateral sensorineural hearing loss; Language delays- communicates through sounds, signs, and screams; Von villebrand disease; Other specific leukocyte disorders, Gastrostomy; Hypothyroidism; Other specified disorders of the kidney and ureter; Other types of infantile paralysis

Listed: Aug 2024

*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***

2025 MACC, Available to Large Families, Available to Single Fathers, Available to Single Mothers

Jaxon has a warm smile and readily shares it with anyone around him. He is also affectionate. He does not like to feel limited or subject to restraints. Jaxon likes to explore and laugh a lot with the people he recognizes as close.

VIDEOS:

https://vimeo.com/maaspecialkids/maa-jaxon01

https://vimeo.com/maaspecialkids/maa-jaxon02

https://vimeo.com/maaspecialkids/maa-jaxon003

https://vimeo.com/maaspecialkids/maa-jaxon004

Password: Adoptmaa

There is a $1,000 agency fee reduction for Jaxon’s adoption, with a specific adoption agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

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